A new view on dam lines in Polish Arabian horses based on mtdna analysis

Size: px
Start display at page:

Download "A new view on dam lines in Polish Arabian horses based on mtdna analysis"

Transcription

1 Genet. Sel. Evol. 39 (2007) c INRA, EDP Sciences, 2007 DOI: /gse: Available online at: Original article A new view on dam lines in Polish Arabian horses based on mtdna analysis Iwona GłAŻEWSKA a, Anna WYSOCKA a,barbaragralak b Renata PRUS a, Jerzy SELL a a Department of Genetics and Cytology, University of Gdańsk, Kładki 24, Gdańsk, Poland b Polish Academy of Sciences Institute of Genetics and Animal Breeding, Jastrzȩbiec, Wólka Kosowska, Poland (Received 5 December 2006; accepted 9 March 2007) Abstract Polish Arabian horses are one of the oldest and the most important Arab populations in the world. The Polish Arabian Stud Book and the Genealogical Charts by Skorkowski are the main sources of information on the ancestors of Polish Arabs. Both publications were viewed as credible sources of information until the 1990s when the data regarding one of the dam lines was questioned. The aim of the current study was to check the accuracy of the pedigree data of Polish dam lines using mtdna analysis. The analyses of a 458 bp mtdna D-loop fragment from representatives of 15 Polish Arabian dam lines revealed 14 distinct haplotypes. The results were inconsistent with pedigree data in the case of two lines. A detailed analysis of the historical sources was performed to explain these discrepancies. Our study revealed that representatives of different lines shared the same haplotypes. We also noted a genetic identity between some lines founded by Polish mares of unknown origin and lines established by desert-bred mares. mitochondrial DNA / horse / pedigree / phylogeny 1. INTRODUCTION Polish Arabian horses are one of the oldest and most important Arab populations in the world. The first stud described in historical sources was established in 1778 [16]. Nineteenth century studs were located in the southeast region of historical Poland, which corresponds now to the Ukrainian territory. The foundation breeding material was of a different origin. The Biała Cerkiew and Sławuta stocks are traced back to local mares, and five dam lines originating from these studs are currently present in Polish breeding (Tab. I). Corresponding author: glazew@biotech.ug.gda.pl Article published by EDP Sciences and available at or

2 610 I. Głażewska et al. Table I. Dam lines in Arabian horses in Poland: founders and main branches of the lines. * In brackets: percentage of representatives of the line of brood mares registered in 2003; db: desert-bred mares. ** In brackets: generation number with the founder generation considered as 0; abbreviations: A: Austro-Hungarian Empire, Radautz stud; PL: Poland; SU-USSR: Tersk stud.

3 Origin of Polish Arabian horses 611 The second group of founders consisted of horses imported from the Near East, and included the mares Gazella, Mlecha, and Sahara, the founders of very valuable dam lines. World War I and the October Revolution resulted in the total destruction of most of the Polish studs [7]. Extensive reconstruction of Polish Arabian breeding was undertaken in the subsequent years, and mares representing the new dam lines of Rodania, Selma, and Cherifa were imported to Polish studs. World War II inflicted another ruinous blow to Polish breeding, during which most of the studs were destroyed, and the horses were either plundered or were missing [13, 14, 16]. Post-war breeding started with 59 surviving brood mares and 14 mares from the Babolna stud [7]. The representatives of four new dam lines were among Babolna s mares (Tab. I), and the Szamrajówka and Rodania lines were revived by importing representatives from the Tersk stud (former USSR). While Polish Arabian breeding started at the end of the 18th century, the history of the Polish studbook dates back to 1926; only a few reports containing incomplete pedigree data were published beforehand [16]. More or less accurate breeding registers were kept in some studs; unfortunately, they were completely destroyed in Efforts to create an official studbook were undertaken in the 1920s and the first studbook, edited by Dr. Edward Skorkowski was published in 1926, which was then revised and published in 1932 as the Polish Arabian Stud Book (PASB), Vol. I. In 1938, Skorkowski published the Genealogical Charts of Polish Arabian horses. Due to the scrupulous work performed by the editor in preparing these charts, both publications were considered for years to be credible sources of information on the ancestors of Polish Arabs. It was not until the 1990s that one of the female lines was called into doubt. According to Kwiatkowski [11], one of two branches of the Milordka line, in fact, originates from the mare Malikarda. Research methods based on mtdna analysis can permit the verification of Kwiatkowski s hypothesis. The verification of dam lines, the history of which was re-created based on incomplete sources, was the second aim of the current study. The third aim of the work was to evaluate the genetic similarity between the founders of the oldest Polish lines, the ancestors of which are unknown, and the founders purchased in the Near East and admitted as purebred Arabian mares.

4 612 I. Głażewska et al. 2. MATERIAL AND METHODS The material analysed comprised peripheral blood samples from 44 randomly chosen representatives of 15 dam lines and their most important branches in Poland (Tab. I). The samples came from the collection for routine testing of parentage controls carried out at the Institute of Genetics and Animal Breeding in Jastrzȩbiec. In 2002, these lines were represented by 98.4% of the total 722 registered brood mares [14]. In addition to the lines analysed in the current study, single representatives of different dam lines imported in recent years are also present in Polish studs. The samples were stored at 20 C. Total DNA was extracted using the Genomic Mini kit (A&A Biotechnology) according to the manufacturer s guidelines. The mtdna D-loop hypervariable region was amplified using the following: forward primer 5 -AACGTTTCCTCCCAAGGACT-3 [4] and reverse primer IRD ATGGCCCTGAAGAAAGAACC-3 [9]. These primers amplify a 458 bp fragment between sites and Amplification of the mitochondrial D-loop region was carried out in a total volume of 20 µl polymerase chain reaction mixture with 1.6 µl dntp(10mm), 2 µl 10XPCRbuffer for Taq DNA Polymerase (Invitrogen), 1 µl MgCl 2 (50 mm), 0.6 µl 5µM of each primer, about 50 ng of template and 0.2 µl Taq DNA Polymerase (5U µl 1, Invitrogen). PCR conditions were as follows:5minat94 C; 35 cycles of the following: 1 min at 94 C, 45 s at 58.5 C, 1 min at 72 C; final extension at 72 C for 10 min. The amplified DNA was electrophoresed in 1% agarose gel containing ethidium bromide to check fragment length. PCR products were sequenced directly in both directions, using the same primers then for amplification. To check the quality of sequencing, BLAST [1] searches were performed. The sequences were aligned using BioEdit [8] and the GenBank X79547 reference sequence [21] was included. Finally, the haplotypes of Polish Arabs were compared to those of Arabian horses in the USA [4] based on the equine mtdna control region between and bp. 3. RESULTS The analyses of a 458 bp mtdna D-loop fragment in representatives of 15 Polish Arabian dam lines identified 14 distinct haplotypes. They differ from the reference sequence (GenBank X79547) by four to ten sites, and altogether by 32 sites as base substitutions (all transitions; Tab. I). Differences between the haplotypes ranged from one to 14 with an average of 9.07 nucleotides.

5 Table II. Variable site positions in the mtdna control region for 14 Polish Arabian horse haplotypes defined by sequence analysis. Dots indicate concordance with the X79547 GenBank sequence; the DNA sequences of all haplotypes are available in GenBank under Acc. No. EF EF Origin of Polish Arabian horses 613

6 614 I. Głażewska et al. Eight haplotypes were each represented in a single dam line. All Babolna s dam lines, Szamrajówka, Selma, and two of four of Sławuta s lines (Szweykowska and Wołoszka) were concerned. Two haplotypes were each shared by representatives of two lines. The G haplotype was found in the Ukrainka and Mlecha lines, and the K haplotype was registered in the Rodania and Cherifa lines. More than one haplotype was found in two lines. The D and E haplotypes, differing from each other by 13 nucleotides, were found in the Milordka line. The D haplotype was identified in the branch established by Zaira, a daughter of Milordka. The E haplotype was found in the branch comprised of approximately 28% of the representatives of the line [14] and founded by Milordka s second daughter, Delfina, whose origin has been questioned by Kwiatkowski [11]. Two haplotypes were also found in the Gazella line. The F haplotype was identified in the branch continued by Gazella II (Tab. I). The second haplotype, which is identical to the H haplotype of the Sahara line, was found in the second branch continued by Fryga. This branch is represented by approximately 35% of the mares from the line. Figure 1 shows the relationships between the haplotypes of Polish and American lines [4]. The analysis yielded four groups of lines with differences not greater than four nucleotides. The largest group includes 16 lines, of which are those founded by Polish mares of unknown origin: Wołoszka, Szweykowska, and Milordka s daughter Zaira. The group of the highest similarity proved to be that of Adjuze, Mlecha, Ukrainka, Szamrajówka and six foreign lines, with differences from one to three nucleotides. Haplotypes identical to those found in American Arabian horses analysed by Bowling et al. were present in eight lines (Fig. 1). Particular attention was given to the genetic identity between the line founded by Szamrajówka, a mare of unknown origin born about 1810, and the line of Balkis, a desert-bred (d.b.) mare imported to France in The genetic identity between the largest Polish line of Gazella d.b. and the line of Murana I d.b., imported in 1816 to the Weil stud (Würtenberg, Germany) is also worth noting. 4. DISCUSSION The current results were inconsistent with pedigree data recorded in the Genealogical Charts by Skorkowski [18] in two cases. A detailed analysis of historical sources was performed to explain these discrepancies. In the case of the Milordka line, the results indicate a possible error in the record of the line, which was suggested by Kwiatkowski [11]. Haplotype D

7 Origin of Polish Arabian horses 615 Figure 1. Relationship among Arabian dam lines based on sequence data of the bp mtdna region. The number of nucleotide substitutions is given; respective values in brackets correspond to the bp fragment. was found in the branch established by Milordka s daughter Zaira 1826 (Tab. I). This haplotype was identical (within the region analysed by Bowling et al. [4]) to the A25 haplotype found in representatives of the Milordka line in the USA. A second haplotype (E) was found in the horses from the branch that originated from Milordka s second daughter, Delfina The difference

8 616 I. Głażewska et al. between the haplotypes is significant and refers to 13 sites, which excludes the common origin of both branches. Considering the accuracy in stud registration and the clear system of foal marking at the Sławuta stud [2], errors regarding the identity of some mares from the line are rather improbable. Errors in reading the hand-written data of the studbook, however, cannot be excluded. In some of the documents from the Sławuta stud, copies of which are in Kwiatkowski s possession, the mare identified by Skorkowski [18] as Milordka daughter Delfina, is registered as Delfinka 1825, the daughter of Malikarda The last record is described in the documents with the annotation z dawnego. This term can be translated as from the old (stud) and can be interpreted to be synonymous with the designation of Malikarda as a founder mare (Kwiatkowski, personal communication). The current findings provide strong evidence for the validity of the hypothesis that there are two independent lines in the present Milordka line. Two haplotypes were also found in the Gazella line. The F haplotype was found in the branch continued by Gazella II born in 1914 in the Jezupol stud and her four daughters. The haplotype is identical, within the region compared, to the A19 haplotype found in the American representatives of the line [4]. The second haplotype (H) was identified in the branch continued by Fryga born in 1914 in the Pełkinie stud and her two daughters. This haplotype is identical to the haplotype found in the Sahara line in both Polish and American (A04 haplotype) horses. The presence of the H haplotype in the Fryga branch undermines the official pedigree data. The analysis of historical sources indicates some possible reasons of the error. Firstly, a proper stud register was not maintained in the Jarczowce stud [16], which might have led to the erroneous reconstruction of the Fryga pedigree. The faulty identification of one of the mare s ancestors is equally probable; after the death of the first owner in 1884, the horses from the Jarczowce stud were divided between his heirs into five studs, including Pełkinie and Jezupol [2]. However, an error in the identification of Fryga during World War I appears to be most probable. The Russian army confiscated almost all the horses from the Pełkinie stud in 1914, and only a few foals were left in the stud, together with Fryga [6]. Without stud data it is impossible to determine precisely the identity of the mare. Nevertheless, on the basis of information from three sources [3, 5, 12], it can be speculated that Fryga was actually a descendant of Sahara s great-granddaughter Mołodycia, whose daughter and two granddaughters were in the stud in The pedigree errors found in the Milordka and Gazella lines concern 11% of the brood mares registered in 2002 in PASB. This number is comparable to the results of the Lipizzan horses analysis, where discrepancies between pedigree

9 Origin of Polish Arabian horses 617 data and mtdna haplotypes were found in 18 of the 56 lines analysed, which also covered about 11% of the population [10]. The occurrence of the same haplotype in two lines is another issue worth consideration. The K haplotype was found in the Rodania and Cherifa lines. There is no reason to question the pedigree data of both lines. The occurrence of this haplotype in different lines was also confirmed by a study of American Arabs [4]. Haplotype A1, the 397 nucleotide-long fragment of the K haplotype, was noted in the Rodania, Wadduda, Urfah, and Noura lines. The same haplotype occurring in five lines may be recognised as evidence of their common origin. The existence of similar haplotypes in different dam lines has also been demonstrated in Lipizzan [10] and Thoroughbred [9] horses. A common haplotype (G) was also found in the Mlecha and Ukrainka lines. The accuracy of the pedigree data of the Mlecha line is beyond all question. The main branches of the line were established by two of Mlecha s daughters (Tab. I). The G haplotype is identical to the A13 haplotype (within the region analysed) found in the American descendants of Mlecha [4]. The Ukrainka line was bred in Sławuta and then in the Gumniska (from the fifth generation) studs until There were no representatives of the Mlecha line in these studs [14, 15], which precludes potential errors in horse identification during stud activity. There is also no convincing evidence to suggest that the only continuator of the line (Forta 1943) was misidentified during wartime ([13, 14, 20], Pankiewicz, personal communication). Furthermore, it should be pointed out that identical haplotypes (within the region compared) were also found in American representatives of the Dahma line [4]. The presence of identical haplotypes in lines established by mares recognised as desert-bred Arabs and in those of unknown origin may be admitted as evidence of the Arabian origin of the latter. Different opinions on the ancestry of foundation stocks in the oldest Polish studs are presented in the historical sources. According to Skorkowski [17], the stocks were comprised of local breeding Tarpan-type mares (so-called Polish mares) that were repeatedly mated by oriental stallions. Bojanowski and Tarnowski [2,19], in turn, reported that the foundation stock of the Biała Cerkiew stud in 1778 was composed of Polish, Persian, and Cherkesian mares. The results of the current study shed new light on the origin of the ancestors of the oldest Polish Arabian dam lines. This issue will be considered fully in the authors next study. It should be emphasised that any size difference in the mtdna region analysed may influence the accuracy of the evaluation of genetic similarity. As shown in Figure 1, there are differences in the number of nucleotides that differentiate particular lines depending on the length of the mtdna control region

10 618 I. Głażewska et al. analysed. For example, the Szweykowska and Wołoszka haplotypes differ by three (397 bp region) or seven sites (458 bp region), while the Szweykowska and Scherife haplotypes vary by three or eight sites, respectively. The current analysis of Polish Arabian dam lines, similarly to those by Hill et al. [9] and Kavar et al. [10], demonstrates the usefulness of mtdna analysis in the verification of historical pedigree records. As Hill et al. justly point out, the findings of such analyses may be of great importance for horse breeders since their decisions often depend on pedigree information. ACKNOWLEDGEMENTS This paper is dedicated to memory of Dr. Edward Skorkowski ( ), the preeminent authority on Polish Arabian horse pedigrees, the first Secretary of the Arab Horse Breeding Society of Poland, the first editor of Polish Arabian Stud Book, and the compiler of Genealogical Charts of Polish Arabian horses. REFERENCES [1] Altshul S.F., Gish W., Miller W., Myers E.W., Lipman D.J., Basic local alignment search tool, J. Mol. Biol. 215 (1990) [2] Bojanowski S., Wycieczka po konie, Jeździec i Myśliwy 6, 13, 20 (1902). [3] Bojanowski S., Sylwetki koni orientalnych i ich hodowców, Kraków, [4] Bowling A.T., Del Valle A., Bowling M., A pedigree-based study of mitochondrial D-loop DNA sequence variation among Arabian horses, Anim. Genet. 31 (2000) 1 7. [5] Czartoryski W., Stado ks. W. Czartoryskiego w Pełkiniach, Jeździec i Myśliwy 13 (1902). [6] Czartoryski W., Stado Pełkińskie, Jeździec i Hodowca 7 (1933) [7] Głażewska I., Jezierski T., Pedigree analysis of Polish Arabian horses based on founder contributions, Livest. Prod. Sci. 90 (2004) [8] Hall T.A., BioEdit: a user - friendly biological sequence alignment editor and analysis program for Windows 95/98/NT (1999), [9] Hill E.W., Bradley D.G., Al-Barody M., Ertugrul O., Splan R.K., Zakahrov I., Cunningham E.P., History and integrity of thoroughbred dam lines revealed in equine mtdna variation, Anim. Genet. 33 (2002) [10] Kavar T., Brem G., Habe F., Sölkner J., Dovč P., History of Lipizzan horse maternal lines as revealed by mtdna analysis, Genet. Sel. Evol. 34 (2002) [11] Kwiatkowski W., A guide to the complete pedigrees of Arabian horses from Poland, Kawalkada Brwinów, [12] Ostaszewski Ostoja K., Oficjalna Ksiȩga Stad koni orientalnych dla Galicji i Bukowiny, Kraków, 1899.

11 Origin of Polish Arabian horses 619 [13] Pankiewicz R., Polska hodowla koni czystej krwi arabskiej , Ed. Petroniusz Frejlich, [14] PASB (Polish Arabian Stud Book) 1932 (vol. I) 2003 (vol. XIV, supp. 2), Present Ed. Polski Klub Wyścigów Konnych Warszawa. [15] Pruski W., Stado arabskie w Gumniskach, Jeździec i Hodowca 12 (1930) [16] Pruski W., Dwa wieki polskiej hodowli koni arabskich ( ) i jej sukcesy na świecie, PWRiL Warszawa, [17] Skorkowski E., Koń arabski w Polsce, Jeździec i Hodowca 31 (1927) [18] Skorkowski E., Tablice genealogiczne polskich koni arabskich czystej krwi, Instytut Zootechniki Kraków, [19] Tarnowski M., Stada hrabiów Branickich, Jeździec i Hodowca 30 (1934) [20] Vetulani T., Wrażenia z wycieczki do Racotu, Hodowca Koni 4 (1946) [21] Xu X., Aranson U., The complete mitochondrial DNA sequence of the horse Equus caballus: extensive heteroplasmy of the control region, Gene 148 (1994)

Formation of a new dog population observed by pedigree and mtdna analyses of the Polish Hovawart

Formation of a new dog population observed by pedigree and mtdna analyses of the Polish Hovawart Archiv Tierzucht 55 (2012) 4, 391-401, ISSN 0003-9438 Leibniz Institute for Farm Animal Biology, Dummerstorf, Germany Formation of a new dog population observed by pedigree and mtdna analyses of the Polish

More information

Heritability of racing merit of Arab horses

Heritability of racing merit of Arab horses Animal Science Papers and Reports vol. 21 (2003) no. 4, 233-239 Institute of Genetics and Animal Breeding, Jastrzębiec, Poland Heritability of racing merit of Arab horses Magdalena Sobczyńska, Marek Łukaszewicz

More information

RT-PCR: Two-Step Protocol

RT-PCR: Two-Step Protocol RT-PCR: Two-Step Protocol We will provide both one-step and two-step protocols for RT-PCR. We recommend the twostep protocol for this class. In the one-step protocol, the components of RT and PCR are mixed

More information

PrimeSTAR HS DNA Polymerase

PrimeSTAR HS DNA Polymerase Cat. # R010A For Research Use PrimeSTAR HS DNA Polymerase Product Manual Table of Contents I. Description...3 II. III. IV. Components...3 Storage...3 Features...3 V. General Composition of PCR Reaction

More information

Troubleshooting for PCR and multiplex PCR

Troubleshooting for PCR and multiplex PCR Page 1 of 5 Page designed and maintained by Octavian Henegariu (Email: Tavi's Yale email or Tavi's Yahoo email). As I am currently pursuing a new junior faculty position, the Yale URL and email may change

More information

Mitochondrial DNA Analysis

Mitochondrial DNA Analysis Mitochondrial DNA Analysis Lineage Markers Lineage markers are passed down from generation to generation without changing Except for rare mutation events They can help determine the lineage (family tree)

More information

ID kit. imegen Anchovies II. and E. japonicus) DNA detection by. User manual. Anchovies species (E. encrasicolus. sequencing.

ID kit. imegen Anchovies II. and E. japonicus) DNA detection by. User manual. Anchovies species (E. encrasicolus. sequencing. User manual imegen Anchovies II ID kit Anchovies species (E. encrasicolus and E. japonicus) DNA detection by sequencing Reference: Made in Spain The information in this guide is subject to change without

More information

Protocols. Internal transcribed spacer region (ITS) region. Niklaus J. Grünwald, Frank N. Martin, and Meg M. Larsen (2013)

Protocols. Internal transcribed spacer region (ITS) region. Niklaus J. Grünwald, Frank N. Martin, and Meg M. Larsen (2013) Protocols Internal transcribed spacer region (ITS) region Niklaus J. Grünwald, Frank N. Martin, and Meg M. Larsen (2013) The nuclear ribosomal RNA (rrna) genes (small subunit, large subunit and 5.8S) are

More information

HiPer RT-PCR Teaching Kit

HiPer RT-PCR Teaching Kit HiPer RT-PCR Teaching Kit Product Code: HTBM024 Number of experiments that can be performed: 5 Duration of Experiment: Protocol: 4 hours Agarose Gel Electrophoresis: 45 minutes Storage Instructions: The

More information

DNA and Forensic Science

DNA and Forensic Science DNA and Forensic Science Micah A. Luftig * Stephen Richey ** I. INTRODUCTION This paper represents a discussion of the fundamental principles of DNA technology as it applies to forensic testing. A brief

More information

A quick and simple method for the identi cation of meat species and meat products by PCR assay

A quick and simple method for the identi cation of meat species and meat products by PCR assay Meat Science 51 (1999) 143±148 A quick and simple method for the identi cation of meat species and meat products by PCR assay T. Matsunaga a, K. Chikuni b *, R. Tanabe b, S. Muroya b, K. Shibata a, J.

More information

Rapid Acquisition of Unknown DNA Sequence Adjacent to a Known Segment by Multiplex Restriction Site PCR

Rapid Acquisition of Unknown DNA Sequence Adjacent to a Known Segment by Multiplex Restriction Site PCR Rapid Acquisition of Unknown DNA Sequence Adjacent to a Known Segment by Multiplex Restriction Site PCR BioTechniques 25:415-419 (September 1998) ABSTRACT The determination of unknown DNA sequences around

More information

Gene Mapping Techniques

Gene Mapping Techniques Gene Mapping Techniques OBJECTIVES By the end of this session the student should be able to: Define genetic linkage and recombinant frequency State how genetic distance may be estimated State how restriction

More information

Lecture 13: DNA Technology. DNA Sequencing. DNA Sequencing Genetic Markers - RFLPs polymerase chain reaction (PCR) products of biotechnology

Lecture 13: DNA Technology. DNA Sequencing. DNA Sequencing Genetic Markers - RFLPs polymerase chain reaction (PCR) products of biotechnology Lecture 13: DNA Technology DNA Sequencing Genetic Markers - RFLPs polymerase chain reaction (PCR) products of biotechnology DNA Sequencing determine order of nucleotides in a strand of DNA > bases = A,

More information

Forensic DNA Testing Terminology

Forensic DNA Testing Terminology Forensic DNA Testing Terminology ABI 310 Genetic Analyzer a capillary electrophoresis instrument used by forensic DNA laboratories to separate short tandem repeat (STR) loci on the basis of their size.

More information

DNA: A Person s Ultimate Fingerprint

DNA: A Person s Ultimate Fingerprint A partnership between the UAB Center for Community Outreach Development and McWane Center DNA: A Person s Ultimate Fingerprint This project is supported by a Science Education Partnership Award (SEPA)

More information

PCR was carried out in a reaction volume of 20 µl using the ABI AmpliTaq GOLD kit (ABI,

PCR was carried out in a reaction volume of 20 µl using the ABI AmpliTaq GOLD kit (ABI, Supplemental Text/Tables PCR Amplification and Sequencing PCR was carried out in a reaction volume of 20 µl using the ABI AmpliTaq GOLD kit (ABI, Foster City, CA). Each PCR reaction contained 20 ng genomic

More information

RevertAid Premium First Strand cdna Synthesis Kit

RevertAid Premium First Strand cdna Synthesis Kit RevertAid Premium First Strand cdna Synthesis Kit #K1651, #K1652 CERTIFICATE OF ANALYSIS #K1651 Lot QUALITY CONTROL RT-PCR using 100 fg of control GAPDH RNA and GAPDH control primers generated a prominent

More information

A Primer of Genome Science THIRD

A Primer of Genome Science THIRD A Primer of Genome Science THIRD EDITION GREG GIBSON-SPENCER V. MUSE North Carolina State University Sinauer Associates, Inc. Publishers Sunderland, Massachusetts USA Contents Preface xi 1 Genome Projects:

More information

Reverse Transcription System

Reverse Transcription System TECHNICAL BULLETIN Reverse Transcription System Instruc ons for use of Product A3500 Revised 1/14 TB099 Reverse Transcription System All technical literature is available on the Internet at: www.promega.com/protocols/

More information

SOP Title: Multiplex-PCR check of genomic DNA isolated from FFPE tissue for its usability in array CGH analysis

SOP Title: Multiplex-PCR check of genomic DNA isolated from FFPE tissue for its usability in array CGH analysis SOP Title: Multiplex-PCR check of genomic DNA isolated from FFPE tissue for its usability in array CGH analysis The STORE processing methods were shown to be fit-for purpose for DNA, RNA and protein extraction

More information

Multiple Losses of Flight and Recent Speciation in Steamer Ducks Tara L. Fulton, Brandon Letts, and Beth Shapiro

Multiple Losses of Flight and Recent Speciation in Steamer Ducks Tara L. Fulton, Brandon Letts, and Beth Shapiro Supplementary Material for: Multiple Losses of Flight and Recent Speciation in Steamer Ducks Tara L. Fulton, Brandon Letts, and Beth Shapiro 1. Supplementary Tables Supplementary Table S1. Sample information.

More information

CCR Biology - Chapter 9 Practice Test - Summer 2012

CCR Biology - Chapter 9 Practice Test - Summer 2012 Name: Class: Date: CCR Biology - Chapter 9 Practice Test - Summer 2012 Multiple Choice Identify the choice that best completes the statement or answers the question. 1. Genetic engineering is possible

More information

ABSTRACT. Promega Corporation, Updated September 2008. http://www.promega.com/pubhub. 1 Campbell-Staton, S.

ABSTRACT. Promega Corporation, Updated September 2008. http://www.promega.com/pubhub. 1 Campbell-Staton, S. A Modified Wizard SV Genomic DNA Purification System Protocol to Purify Genomic DNA... A Modified Wizard SV Genomic DNA Purification System Protocol to Purify Genomic DNA from Shed Reptile Skin ABSTRACT

More information

The impact of genomic selection on North American dairy cattle breeding organizations

The impact of genomic selection on North American dairy cattle breeding organizations The impact of genomic selection on North American dairy cattle breeding organizations Jacques Chesnais, George Wiggans and Filippo Miglior The Semex Alliance, USDA and Canadian Dairy Network 2000 09 Genomic

More information

Amazing DNA facts. Hands-on DNA: A Question of Taste Amazing facts and quiz questions

Amazing DNA facts. Hands-on DNA: A Question of Taste Amazing facts and quiz questions Amazing DNA facts These facts can form the basis of a quiz (for example, how many base pairs are there in the human genome?). Students should be familiar with most of this material, so the quiz could be

More information

Introduction to the Horse Racing Industry

Introduction to the Horse Racing Industry Unit 19: Introduction to the Horse Racing Industry Unit code: QCF Level 3: Credit value: 10 Guided learning hours: 60 Aim and purpose R/601/1520 BTEC National This unit aims to provide learners with an

More information

Use of the Agilent 2100 Bioanalyzer and the DNA 500 LabChip in the Analysis of PCR Amplified Mitochondrial DNA Application

Use of the Agilent 2100 Bioanalyzer and the DNA 500 LabChip in the Analysis of PCR Amplified Mitochondrial DNA Application Use of the Agilent 2100 Bioanalyzer and the DNA LabChip in the Analysis of PCR Amplified Mitochondrial DNA Application Homeland Security/Forensics Author Mark Jensen Agilent Technologies, Inc. 2850 Centerville

More information

Annex to the Accreditation Certificate D-PL-13372-01-00 according to DIN EN ISO/IEC 17025:2005

Annex to the Accreditation Certificate D-PL-13372-01-00 according to DIN EN ISO/IEC 17025:2005 Deutsche Akkreditierungsstelle GmbH German Accreditation Body Annex to the Accreditation Certificate D-PL-13372-01-00 according to DIN EN ISO/IEC 17025:2005 Period of validity: 26.03.2012 to 25.03.2017

More information

PyroPhage 3173 DNA Polymerase, Exonuclease Minus (Exo-)

PyroPhage 3173 DNA Polymerase, Exonuclease Minus (Exo-) PyroPhage 3173 DNA Polymerase, Exonuclease Minus (Exo-) FOR RESEARCH USE ONLY. NOT FOR HUMAN OR DIAGNOSTIC USE Lucigen Corporation 2905 Parmenter St, Middleton, WI 53562 USA Toll Free: (888) 575-9695 (608)

More information

Regulations for Record Keeping and Identification of Dogs

Regulations for Record Keeping and Identification of Dogs Regulations for Record Keeping and Identification of Dogs Amended to August 2005 Also Applies to Foundation Stock Service The regulations contained herein have been promulgated by the Board of Directors

More information

Intended Use: The kit is designed to detect the 5 different mutations found in Asian population using seven different primers.

Intended Use: The kit is designed to detect the 5 different mutations found in Asian population using seven different primers. Unzipping Genes MBPCR014 Beta-Thalassemia Detection Kit P r o d u c t I n f o r m a t i o n Description: Thalassemia is a group of genetic disorders characterized by quantitative defects in globin chain

More information

Real-Time PCR Vs. Traditional PCR

Real-Time PCR Vs. Traditional PCR Real-Time PCR Vs. Traditional PCR Description This tutorial will discuss the evolution of traditional PCR methods towards the use of Real-Time chemistry and instrumentation for accurate quantitation. Objectives

More information

Cloning Blunt-End Pfu DNA Polymerase- Generated PCR Fragments into pgem -T Vector Systems

Cloning Blunt-End Pfu DNA Polymerase- Generated PCR Fragments into pgem -T Vector Systems Promega Notes Number 71, 1999, p. 10 Blunt-End Pfu DNA Polymerase- Generated PCR Fragments into pgem -T Vector Systems By Kimberly Knoche, Ph.D., and Dan Kephart, Ph.D. Promega Corporation Corresponding

More information

Interstallion workshop

Interstallion workshop Interstallion workshop Warendorf 5 6 th of september 2005 Xavier Guibert Haras Nationaux 1 General management of horse industry in France Racing authorities France galop French trotter SECF Mutual bettings

More information

The Techniques of Molecular Biology: Forensic DNA Fingerprinting

The Techniques of Molecular Biology: Forensic DNA Fingerprinting Revised Fall 2011 The Techniques of Molecular Biology: Forensic DNA Fingerprinting The techniques of molecular biology are used to manipulate the structure and function of molecules such as DNA and proteins

More information

GENOTYPING ASSAYS AT ZIRC

GENOTYPING ASSAYS AT ZIRC GENOTYPING ASSAYS AT ZIRC A. READ THIS FIRST - DISCLAIMER Dear ZIRC user, We now provide detailed genotyping protocols for a number of zebrafish lines distributed by ZIRC. These protocols were developed

More information

ab185916 Hi-Fi cdna Synthesis Kit

ab185916 Hi-Fi cdna Synthesis Kit ab185916 Hi-Fi cdna Synthesis Kit Instructions for Use For cdna synthesis from various RNA samples This product is for research use only and is not intended for diagnostic use. Version 1 Last Updated 1

More information

Genetic polymorphism of Hucul horse population based on 17 microsatellite loci*

Genetic polymorphism of Hucul horse population based on 17 microsatellite loci* Regular paper Vol. 60, No 4/2013 761 765 on-line at: www.actabp.pl Genetic polymorphism of Hucul horse population based on 17 microsatellite loci* Agnieszka Fornal *, Anna Radko and Agata Piestrzyńska-Kajtoch

More information

Data Analysis for Ion Torrent Sequencing

Data Analysis for Ion Torrent Sequencing IFU022 v140202 Research Use Only Instructions For Use Part III Data Analysis for Ion Torrent Sequencing MANUFACTURER: Multiplicom N.V. Galileilaan 18 2845 Niel Belgium Revision date: August 21, 2014 Page

More information

Terra PCR Direct Polymerase Mix User Manual

Terra PCR Direct Polymerase Mix User Manual Clontech Laboratories, Inc. Terra PCR Direct Polymerase Mix User Manual Cat. Nos. 639269, 639270, 639271 PT5126-1 (031416) Clontech Laboratories, Inc. A Takara Bio Company 1290 Terra Bella Avenue, Mountain

More information

GenScript BloodReady TM Multiplex PCR System

GenScript BloodReady TM Multiplex PCR System GenScript BloodReady TM Multiplex PCR System Technical Manual No. 0174 Version 20040915 I Description.. 1 II Applications 2 III Key Features.. 2 IV Shipping and Storage. 2 V Simplified Procedures. 2 VI

More information

Y Chromosome Markers

Y Chromosome Markers Y Chromosome Markers Lineage Markers Autosomal chromosomes recombine with each meiosis Y and Mitochondrial DNA does not This means that the Y and mtdna remains constant from generation to generation Except

More information

Improved methods for site-directed mutagenesis using Gibson Assembly TM Master Mix

Improved methods for site-directed mutagenesis using Gibson Assembly TM Master Mix CLONING & MAPPING DNA CLONING DNA AMPLIFICATION & PCR EPIGENETICS RNA ANALYSIS Improved methods for site-directed mutagenesis using Gibson Assembly TM Master Mix LIBRARY PREP FOR NET GEN SEQUENCING PROTEIN

More information

Rethinking Polynesian Origins: Human Settlement of the Pacific

Rethinking Polynesian Origins: Human Settlement of the Pacific LENScience Senior Biology Seminar Series Rethinking Polynesian Origins: Human Settlement of the Pacific Michal Denny, and Lisa Matisoo-Smith Our Polynesian ancestors are renowned as some of the world s

More information

Molecular and Cell Biology Laboratory (BIOL-UA 223) Instructor: Ignatius Tan Phone: 212-998-8295 Office: 764 Brown Email: ignatius.tan@nyu.

Molecular and Cell Biology Laboratory (BIOL-UA 223) Instructor: Ignatius Tan Phone: 212-998-8295 Office: 764 Brown Email: ignatius.tan@nyu. Molecular and Cell Biology Laboratory (BIOL-UA 223) Instructor: Ignatius Tan Phone: 212-998-8295 Office: 764 Brown Email: ignatius.tan@nyu.edu Course Hours: Section 1: Mon: 12:30-3:15 Section 2: Wed: 12:30-3:15

More information

BLOODLINE. 220 TUTTO ARABI - www.tuttoarabi.com

BLOODLINE. 220 TUTTO ARABI - www.tuttoarabi.com Skowronek, painted by Andrzej Novak-Zempliński, 2004. From Mr. Marek Potocki s collection photo: Monika Luft design: polskiearaby.com 220 TUTTO ARABI - www.tuttoarabi.com 235 years of Polish private Arabian

More information

Procedures For DNA Sequencing

Procedures For DNA Sequencing Procedures For DNA Sequencing Plant-Microbe Genomics Facility (PMGF) Ohio State University 420 Biological Sciences Building 484 W. 12th Ave., Columbus OH 43210 Telephone: 614/247-6204 FAX: 614/292-6337

More information

Crime Scenes and Genes

Crime Scenes and Genes Glossary Agarose Biotechnology Cell Chromosome DNA (deoxyribonucleic acid) Electrophoresis Gene Micro-pipette Mutation Nucleotide Nucleus PCR (Polymerase chain reaction) Primer STR (short tandem repeats)

More information

RETRIEVING SEQUENCE INFORMATION. Nucleotide sequence databases. Database search. Sequence alignment and comparison

RETRIEVING SEQUENCE INFORMATION. Nucleotide sequence databases. Database search. Sequence alignment and comparison RETRIEVING SEQUENCE INFORMATION Nucleotide sequence databases Database search Sequence alignment and comparison Biological sequence databases Originally just a storage place for sequences. Currently the

More information

Gene Expression Assays

Gene Expression Assays APPLICATION NOTE TaqMan Gene Expression Assays A mpl i fic ationef ficienc yof TaqMan Gene Expression Assays Assays tested extensively for qpcr efficiency Key factors that affect efficiency Efficiency

More information

Supplementary Information - PCR amplification PCR amplification reactions for the partial mitochondrial cytochrome oxidase subunit I (COI), the

Supplementary Information - PCR amplification PCR amplification reactions for the partial mitochondrial cytochrome oxidase subunit I (COI), the Supplementary Information - PCR amplification PCR amplification reactions for the partial mitochondrial cytochrome oxidase subunit I (COI), the ribosomal 16S rdna gene and a fragment of the nuclear single

More information

DNA Sequencing Overview

DNA Sequencing Overview DNA Sequencing Overview DNA sequencing involves the determination of the sequence of nucleotides in a sample of DNA. It is presently conducted using a modified PCR reaction where both normal and labeled

More information

mircute mirna qpcr Detection Kit (SYBR Green)

mircute mirna qpcr Detection Kit (SYBR Green) mircute mirna qpcr Detection Kit (SYBR Green) For detection of mirna using real-time RT-PCR (SYBR Green I) www.tiangen.com QP110302 mircute mirna qpcr Detection Kit (SYBR Green) Kit Contents Cat. no. FP401

More information

A greedy algorithm for the DNA sequencing by hybridization with positive and negative errors and information about repetitions

A greedy algorithm for the DNA sequencing by hybridization with positive and negative errors and information about repetitions BULLETIN OF THE POLISH ACADEMY OF SCIENCES TECHNICAL SCIENCES, Vol. 59, No. 1, 2011 DOI: 10.2478/v10175-011-0015-0 Varia A greedy algorithm for the DNA sequencing by hybridization with positive and negative

More information

IIID 14. Biotechnology in Fish Disease Diagnostics: Application of the Polymerase Chain Reaction (PCR)

IIID 14. Biotechnology in Fish Disease Diagnostics: Application of the Polymerase Chain Reaction (PCR) IIID 14. Biotechnology in Fish Disease Diagnostics: Application of the Polymerase Chain Reaction (PCR) Background Infectious diseases caused by pathogenic organisms such as bacteria, viruses, protozoa,

More information

Mir-X mirna First-Strand Synthesis Kit User Manual

Mir-X mirna First-Strand Synthesis Kit User Manual User Manual Mir-X mirna First-Strand Synthesis Kit User Manual United States/Canada 800.662.2566 Asia Pacific +1.650.919.7300 Europe +33.(0)1.3904.6880 Japan +81.(0)77.543.6116 Clontech Laboratories, Inc.

More information

1/12 Dideoxy DNA Sequencing

1/12 Dideoxy DNA Sequencing 1/12 Dideoxy DNA Sequencing Dideoxy DNA sequencing utilizes two steps: PCR (polymerase chain reaction) amplification of DNA using dideoxy nucleoside triphosphates (Figures 1 and 2)and denaturing polyacrylamide

More information

BacReady TM Multiplex PCR System

BacReady TM Multiplex PCR System BacReady TM Multiplex PCR System Technical Manual No. 0191 Version 10112010 I Description.. 1 II Applications 2 III Key Features.. 2 IV Shipping and Storage. 2 V Simplified Procedures. 2 VI Detailed Experimental

More information

STA DARD OPERATI G PROCEDURE FOR THE DETECTIO OF AFRICA SWI E FEVER VIRUS (ASFV) BY CO VE TIO AL POLYMERASE CHAI REACTIO (PCR)

STA DARD OPERATI G PROCEDURE FOR THE DETECTIO OF AFRICA SWI E FEVER VIRUS (ASFV) BY CO VE TIO AL POLYMERASE CHAI REACTIO (PCR) STA DARD OPERATI G PROCEDURE FOR THE DETECTIO OF AFRICA SWI E FEVER VIRUS (ASFV) BY CO VE TIO AL POLYMERASE CHAI REACTIO (PCR) jmvizcaino@vet.ucm.es Av/ Puerta de Hierro s/n. 28040 Madrid. Tel: (34) 913944082

More information

Recombinant DNA & Genetic Engineering. Tools for Genetic Manipulation

Recombinant DNA & Genetic Engineering. Tools for Genetic Manipulation Recombinant DNA & Genetic Engineering g Genetic Manipulation: Tools Kathleen Hill Associate Professor Department of Biology The University of Western Ontario Tools for Genetic Manipulation DNA, RNA, cdna

More information

NimbleGen DNA Methylation Microarrays and Services

NimbleGen DNA Methylation Microarrays and Services NimbleGen DNA Methylation Microarrays and Services Sample Preparation Instructions Outline This protocol describes the process for preparing samples for NimbleGen DNA Methylation microarrays using the

More information

Application Guide... 2

Application Guide... 2 Protocol for GenomePlex Whole Genome Amplification from Formalin-Fixed Parrafin-Embedded (FFPE) tissue Application Guide... 2 I. Description... 2 II. Product Components... 2 III. Materials to be Supplied

More information

Just the Facts: A Basic Introduction to the Science Underlying NCBI Resources

Just the Facts: A Basic Introduction to the Science Underlying NCBI Resources 1 of 8 11/7/2004 11:00 AM National Center for Biotechnology Information About NCBI NCBI at a Glance A Science Primer Human Genome Resources Model Organisms Guide Outreach and Education Databases and Tools

More information

Reduced-Median-Network Analysis of Complete Mitochondrial DNA Coding-Region Sequences for the Major African, Asian, and European Haplogroups

Reduced-Median-Network Analysis of Complete Mitochondrial DNA Coding-Region Sequences for the Major African, Asian, and European Haplogroups Am. J. Hum. Genet. 70:1152 1171, 2002 Reduced-Median-Network Analysis of Complete Mitochondrial DNA Coding-Region Sequences for the Major African, Asian, and European Haplogroups Corinna Herrnstadt, 1

More information

DNA MARKERS FOR ASEASONALITY AND MILK PRODUCTION IN SHEEP. R. G. Mateescu and M.L. Thonney

DNA MARKERS FOR ASEASONALITY AND MILK PRODUCTION IN SHEEP. R. G. Mateescu and M.L. Thonney DNA MARKERS FOR ASEASONALITY AND MILK PRODUCTION IN SHEEP Introduction R. G. Mateescu and M.L. Thonney Department of Animal Science Cornell University Ithaca, New York Knowledge about genetic markers linked

More information

Introduction. Preparation of Template DNA

Introduction. Preparation of Template DNA Procedures and Recommendations for DNA Sequencing at the Plant-Microbe Genomics Facility Ohio State University Biological Sciences Building Room 420, 484 W. 12th Ave., Columbus OH 43210 Telephone: 614/247-6204;

More information

2. True or False? The sequence of nucleotides in the human genome is 90.9% identical from one person to the next. False (it s 99.

2. True or False? The sequence of nucleotides in the human genome is 90.9% identical from one person to the next. False (it s 99. 1. True or False? A typical chromosome can contain several hundred to several thousand genes, arranged in linear order along the DNA molecule present in the chromosome. True 2. True or False? The sequence

More information

The Sport of Thoroughbred Horseracing. Response to the Gambling Review Commission s report

The Sport of Thoroughbred Horseracing. Response to the Gambling Review Commission s report P.O. Box 827, Germiston, 1400 Tel: +27 (011)323 5700 Fax: +27 (011) 323 5788 / 99 E-mail: enquiries@tba.co.za The Sport of Thoroughbred Horseracing Response to the Gambling Review Commission s report The

More information

quantitative real-time PCR, grain, simplex DNA extraction: PGS0426 RT-PCR: PGS0494 & PGS0476

quantitative real-time PCR, grain, simplex DNA extraction: PGS0426 RT-PCR: PGS0494 & PGS0476 BioScience quantitative real-time PCR, grain, simplex DNA extraction: PGS0426 RT-PCR: PGS0494 & PGS0476 This method describes a Real-time semi-quantitative TaqMan PCR procedure for the determination of

More information

Taq98 Hot Start 2X Master Mix

Taq98 Hot Start 2X Master Mix Taq98 Hot Start 2X Master Mix Optimized for 98C Denaturation Lucigen Corporation 2905 Parmenter St, Middleton, WI 53562 USA Toll Free: (888) 575-9695 (608) 831-9011 FAX: (608) 831-9012 lucigen@lucigen.com

More information

Global MicroRNA Amplification Kit

Global MicroRNA Amplification Kit Global MicroRNA Amplification Kit Store kit at -20 C on receipt (ver. 3-060901) A limited-use label license covers this product. By use of this product, you accept the terms and conditions outlined in

More information

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome 1998 Oxford University Press Nucleic Acids Research, 1998, Vol. 26, No. 4 967 973 Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial

More information

The RNAi Consortium (TRC) Broad Institute

The RNAi Consortium (TRC) Broad Institute TRC Laboratory Protocols Protocol Title: One Step PCR Preparation of Samples for Illumina Sequencing Current Revision Date: 11/10/2012 RNAi Platform,, trc_info@broadinstitute.org Brief Description: This

More information

Healthy puppies come from breeders who:

Healthy puppies come from breeders who: If you re looking for a new dog, check your local RSPCA or other animal rescue group first. There are many wonderful puppies and dogs out there looking for new homes. But if you can t find the right dog

More information

HISTO TYPE SSP Immunogenetic Diagnostics. Robust and fast - validated Taq Polymerase included

HISTO TYPE SSP Immunogenetic Diagnostics. Robust and fast - validated Taq Polymerase included HISTO TYPE SSP Immunogenetic Diagnostics Robust and fast - validated Taq Polymerase included BAG Health Care the experts for HLA and blood group diagnostics HISTO TYPE SSP Diagnostics Highly standardised

More information

360 Master Mix. , and a supplementary 360 GC Enhancer.

360 Master Mix. , and a supplementary 360 GC Enhancer. Product Bulletin AmpliTaq Gold 360 Master Mix and 360 DNA Polymerase AmpliTaq Gold 360 Master Mix AmpliTaq Gold 360 DNA Polymerase 360 Coverage for a Full Range of Targets AmpliTaq Gold 360 Master Mix

More information

FORENSIC SCIENCE COURSE DESCRIPTION

FORENSIC SCIENCE COURSE DESCRIPTION FORENSIC SCIENCE COURSE DESCRIPTION This course is an overview of how science is applied to solving crimes. Topics include history of forensic sciences, collecting of evidence, analyzing results and hands-on

More information

QUANTITATIVE RT-PCR. A = B (1+e) n. A=amplified products, B=input templates, n=cycle number, and e=amplification efficiency.

QUANTITATIVE RT-PCR. A = B (1+e) n. A=amplified products, B=input templates, n=cycle number, and e=amplification efficiency. QUANTITATIVE RT-PCR Application: Quantitative RT-PCR is used to quantify mrna in both relative and absolute terms. It can be applied for the quantification of mrna expressed from endogenous genes, and

More information

Genetic Technology. Name: Class: Date: Multiple Choice Identify the choice that best completes the statement or answers the question.

Genetic Technology. Name: Class: Date: Multiple Choice Identify the choice that best completes the statement or answers the question. Name: Class: Date: Genetic Technology Multiple Choice Identify the choice that best completes the statement or answers the question. 1. An application of using DNA technology to help environmental scientists

More information

PicoMaxx High Fidelity PCR System

PicoMaxx High Fidelity PCR System PicoMaxx High Fidelity PCR System Instruction Manual Catalog #600420 (100 U), #600422 (500 U), and #600424 (1000 U) Revision C Research Use Only. Not for Use in Diagnostic Procedures. 600420-12 LIMITED

More information

Development of two Novel DNA Analysis methods to Improve Workflow Efficiency for Challenging Forensic Samples

Development of two Novel DNA Analysis methods to Improve Workflow Efficiency for Challenging Forensic Samples Development of two Novel DNA Analysis methods to Improve Workflow Efficiency for Challenging Forensic Samples Sudhir K. Sinha, Ph.D.*, Anne H. Montgomery, M.S., Gina Pineda, M.S., and Hiromi Brown, Ph.D.

More information

Authentication of Basmati rice using SSR-PCR and QIAxcel Advanced

Authentication of Basmati rice using SSR-PCR and QIAxcel Advanced Application Note Authentication of Basmati rice using SSR-PCR and QIAxcel Advanced R. Cassier ADGENE Laboratoire, Thury Harcourt, France Introduction Basmati is one of the most popular types of rice in

More information

DNA Integrity Number (DIN) For the Assessment of Genomic DNA Samples in Real-Time Quantitative PCR (qpcr) Experiments

DNA Integrity Number (DIN) For the Assessment of Genomic DNA Samples in Real-Time Quantitative PCR (qpcr) Experiments DNA Integrity Number () For the Assessment of Genomic DNA Samples in Real-Time Quantitative PCR (qpcr) Experiments Application Note Nucleic Acid Analysis Author Arunkumar Padmanaban Agilent Technologies,

More information

Table of Contents. I. Description... 2. II. Kit Components... 2. III. Storage... 2. IV. 1st Strand cdna Synthesis Reaction... 3

Table of Contents. I. Description... 2. II. Kit Components... 2. III. Storage... 2. IV. 1st Strand cdna Synthesis Reaction... 3 Table of Contents I. Description... 2 II. Kit Components... 2 III. Storage... 2 IV. 1st Strand cdna Synthesis Reaction... 3 V. RT-PCR, Real-time RT-PCR... 4 VI. Application... 5 VII. Preparation of RNA

More information

The sample is taken with a simple mouth swab no blood is involved. There will be instructions included on how to take the sample.

The sample is taken with a simple mouth swab no blood is involved. There will be instructions included on how to take the sample. DNA testing Thanks for your enquiry about DNA testing. I oversee the Scottish DNA Project on behalf of the University of Strathclyde, Glasgow and act as representative for Family Tree DNA who host our

More information

Sequencing Guidelines Adapted from ABI BigDye Terminator v3.1 Cycle Sequencing Kit and Roswell Park Cancer Institute Core Laboratory website

Sequencing Guidelines Adapted from ABI BigDye Terminator v3.1 Cycle Sequencing Kit and Roswell Park Cancer Institute Core Laboratory website Biomolecular Core Facility AI Dupont Hospital for Children, Rockland Center One, Room 214 Core: (302) 651-6712, Office: (302) 651-6707, mbcore@nemours.org Katia Sol-Church, Ph.D., Director Jennifer Frenck

More information

DNA Fingerprinting. Unless they are identical twins, individuals have unique DNA

DNA Fingerprinting. Unless they are identical twins, individuals have unique DNA DNA Fingerprinting Unless they are identical twins, individuals have unique DNA DNA fingerprinting The name used for the unambiguous identifying technique that takes advantage of differences in DNA sequence

More information

AMERICAN GENEALOGY: HOME STUDY COURSE

AMERICAN GENEALOGY: HOME STUDY COURSE AMERICAN GENEALOGY: HOME STUDY COURSE Syllabus NGS AMERICAN GENEALOGY HOME STUDY COURSE SYLLABUS Copyright 2009 National Genealogical Society 3108 Columbia Pike, Suite 300 Arlington, Virginia 22204-4370

More information

Identification of the VTEC serogroups mainly associated with human infections by conventional PCR amplification of O-associated genes

Identification of the VTEC serogroups mainly associated with human infections by conventional PCR amplification of O-associated genes Identification of the VTEC serogroups mainly associated with human infections by conventional PCR amplification of O-associated genes 1. Aim and field of application The present method concerns the identification

More information

DNA Sequence Analysis

DNA Sequence Analysis DNA Sequence Analysis Two general kinds of analysis Screen for one of a set of known sequences Determine the sequence even if it is novel Screening for a known sequence usually involves an oligonucleotide

More information

POLISH JOCKEY CLUB. International races in Poland WARSAW SŁUŻEWIEC 2016 (turf)

POLISH JOCKEY CLUB. International races in Poland WARSAW SŁUŻEWIEC 2016 (turf) Day 31, Sunday 21 st of August POLISH JOCKEY CLUB International races in Poland WARSAW SŁUŻEWIEC 2016 (turf) Pure Bred Arabian horses flat races early entries Race no 1 - SHEIKH ZAYED BIN SULTAN AL NAHYAN

More information

Hepatitis B Virus Genemer Mix

Hepatitis B Virus Genemer Mix Product Manual Hepatitis B Virus Genemer Mix Primer Pair for amplification of HBV Specific DNA Fragment Includes Internal Negative Control Primers and Template Catalog No.: 60-2007-12 Store at 20 o C For

More information

Isolation and characterization of nine microsatellite loci in the Pale Pitcher Plant. MARGARET M. KOOPMAN*, ELIZABETH GALLAGHER, and BRYAN C.

Isolation and characterization of nine microsatellite loci in the Pale Pitcher Plant. MARGARET M. KOOPMAN*, ELIZABETH GALLAGHER, and BRYAN C. Page 1 of 28 1 1 2 3 PERMANENT GENETIC RESOURCES Isolation and characterization of nine microsatellite loci in the Pale Pitcher Plant Sarracenia alata (Sarraceniaceae). 4 5 6 MARGARET M. KOOPMAN*, ELIZABETH

More information

Technical Note. Roche Applied Science. No. LC 18/2004. Assay Formats for Use in Real-Time PCR

Technical Note. Roche Applied Science. No. LC 18/2004. Assay Formats for Use in Real-Time PCR Roche Applied Science Technical Note No. LC 18/2004 Purpose of this Note Assay Formats for Use in Real-Time PCR The LightCycler Instrument uses several detection channels to monitor the amplification of

More information

Are you collecting all the available DNA from touched objects?

Are you collecting all the available DNA from touched objects? International Congress Series 1239 (2003) 803 807 Are you collecting all the available DNA from touched objects? R.A.H. van Oorschot a, *, D.G. Phelan a,b, S. Furlong a,b, G.M. Scarfo a,b, N.L. Holding

More information

CURRICULUM GUIDE. When this Forensics course has been completed successfully, students should be able to:

CURRICULUM GUIDE. When this Forensics course has been completed successfully, students should be able to: CURRICULUM GUIDE NAME OF COURSE: FORENSICS COURSE NUMBER: SCI 40 WRITTEN / REVISED: SEPTEMBER, 2011 LEVEL OF COURSE: REPLACMENT NUMBER OF CREDITS: SIX (6) PREREQUISITES: BIOLOGY GRADE LEVELS OFFERED TO:

More information

Appendix 2 Molecular Biology Core Curriculum. Websites and Other Resources

Appendix 2 Molecular Biology Core Curriculum. Websites and Other Resources Appendix 2 Molecular Biology Core Curriculum Websites and Other Resources Chapter 1 - The Molecular Basis of Cancer 1. Inside Cancer http://www.insidecancer.org/ From the Dolan DNA Learning Center Cold

More information

The Chinese University of Hong Kong School of Life Sciences Biochemistry Program CUGEN Ltd.

The Chinese University of Hong Kong School of Life Sciences Biochemistry Program CUGEN Ltd. The Chinese University of Hong Kong School of Life Sciences Biochemistry Program CUGEN Ltd. DNA Forensic and Agarose Gel Electrophoresis 1 OBJECTIVES Prof. Stephen K.W. Tsui, Dr. Patrick Law and Miss Fion

More information

Validation and Replication

Validation and Replication Validation and Replication Overview Definitions of validation and replication Difficulties and limitations Working examples from our group and others Why? False positive results still occur. even after

More information